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Summary Literature (1)
MIM:182212 - SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS

Xenbase Genes: fbn1, ski

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008426 - Shprintzen-Goldberg syndrome

Disease Ontology (DO):
DOID:2340 - craniosynostosis